Constant Volume and Constant Pressure Batch Reactor

AI Thread Summary
The discussion centers on two types of batch reactors for the decomposition of A to B, one with constant volume and variable pressure, and the other with constant pressure and variable volume. For the constant volume reactor, the fractional decrease in concentration of A can be calculated using the first-order reaction formula, resulting in a straightforward exponential decay. The variable volume reactor presents a challenge, requiring the application of the ideal gas law and a Laplacian transform to derive the concentration over time. Participants suggest that the concentration equation will involve an error function, indicating a more complex integration process. Overall, the problem highlights the differences in approach required for analyzing batch reactors under varying conditions.
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Homework Statement


Consider the following two well-mixed, isothermal batch reactors for the elementary and irreversible decomposition of A to B, A\stackrel{k}{\rightarrow}2B
reactor1: The reactor volume is constant (Pressure is variable)
reactor2: The reactor pressure is constant (Volume is variable)
Both reactors are charged with pure A at 1.0 atm and k=0.35min^{-1}

a) what is the fractional decrease in the concentration of A in reactors 1 and 2 after 5 minutes?
b)what is the total molar conversion of A in reactors 1 and 2 after 5 minutes?



Homework Equations



Since reaction is first order: r_{A}=-kC_{A}

The Attempt at a Solution



Ok, so part a for a constant volume reactor was simple, since the ODE was easy and it turned out that \frac{C_{A}}{C_{A0}}=exp(-kt)
but variable volume has me stumped. I figured out that -k=\frac{dC_{A}}{dt}+(\frac{1}{V})(\frac{dV}{dt} but i don't know where to go from here.

I don't even know where to start for part b, please help...
 
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This problem is a bit complicated, but I remember it from my days as an undergraduate. You have to use a Laplacian transform of the Ideal Gas equation (assuming that T is high enough at 1atm to support this assumption). This should give you an equation for concentration in the form of a Gaussian, which, when integrated, will give an error function. You should work this out for yourself, but your answer should be of the form:

Ca / Cao = erf(-Vr * k * t)

Hope this helps.
 
I'm not sure i understand what exactly you mean, could you spell it out stepwise?
 
just kidding. You actually use the Ideal gas equation and (think about the assumptions made for the ideal gas law) calculate delta(V). Then, think about what Cj means
 
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